Alpha-fetoprotein mediated targeting of polymeric nanoparticles to treat solid tumors

Author:

Sokol Mariya B12ORCID,Yabbarov Nikita G12ORCID,Mollaeva Mariia R12ORCID,Chirkina Margarita V12ORCID,Mollaev Murad D23ORCID,Zabolotsky Artur I24ORCID,Kuznetsov Sergey L5ORCID,Nikolskaya Elena D12ORCID

Affiliation:

1. NM Emanuel Institute of Biochemical Physics of Russian Academy of Sciences, Moscow, 119334, Russia

2. JSC Russian Research Center for Molecular Diagnostics and Therapy, Moscow, 117149, Russia

3. Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, 117198, Russia

4. Lomonosov Moscow State University, Biological Faculty, Department of Biochemistry, Moscow, 119991, Russia

5. National Research Center Kurchatov Institute, Moscow, 123182, Russia

Abstract

Background: Serious side effects caused by paclitaxel formulation, containing toxic solubilizer Cremophor® EL, and its nonspecific accumulation greatly limit clinical paclitaxel application. Aim: To design paclitaxel-loaded copolymer of lactic and glycolic acids nanoparticles decorated with alpha-fetoprotein third domain (rAFP3d-NP) to increase paclitaxel safety profile. Methods: rAFP3d-NP was obtained via carbodiimide technique. Results: The particles were characterized with high paclitaxel loading content of 5% and size of 280 nm. rAFP3d-NP revealed biphasic profile with 67% release of paclitaxel during 220 h. Increased area under the curveinf and mean residence time values after rAFP3d-NP administration confirmed prolonged blood circulation compared with paclitaxel. rAFP3d-NP demonstrated significant tumor growth inhibition at 4T1 and SKOV-3 models. Conclusion: rAFP3d-NP is a promising delivery system for paclitaxel and can be applied similarly for delivery of other hydrophobic drugs.

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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